Victor Dubowitz

Affiliations: 
Imperial College, London, London, England, United Kingdom 
Area:
Paediatric Neurology
Website:
http://en.wikipedia.org/wiki/Victor_Dubowitz
Google:
"Victor Dubowitz"
Mean distance: 29.89 (cluster 44)
 
BETA: Related publications

Publications

You can help our author matching system! If you notice any publications incorrectly attributed to this author, please sign in and mark matches as correct or incorrect.

Dubowitz V. (2005) A short history of the World Muscle Society. Neuromuscular Disorders : Nmd. 15: 642-7
Dubowitz V. (2005) Prednisone for Duchenne muscular dystrophy. The Lancet. Neurology. 4: 264
Dubowitz V. (2004) Therapeutic efforts in Duchenne muscular dystrophy; the need for a common language between basic scientists and clinicians. Neuromuscular Disorders : Nmd. 14: 451-5
Mercuri E, Brockington M, Straub V, et al. (2003) Phenotypic spectrum associated with mutations in the fukutin-related protein gene. Annals of Neurology. 53: 537-42
Tonini MM, Passos-Bueno MR, Cerqueira A, et al. (2002) Facioscapulohumeral (FSHD1) and other forms of muscular dystrophy in the same family: is there more in muscular dystrophy than meets the eye? Neuromuscular Disorders : Nmd. 12: 554-7
Philpot J, Counsell S, Bydder G, et al. (2001) Neonatal arthrogryposis and absent limb muscles: a muscle developmental gene defect? Neuromuscular Disorders : Nmd. 11: 489-93
Jungbluth H, Sewry CA, Brown SC, et al. (2001) Mild phenotype of nemaline myopathy with sleep hypoventilation due to a mutation in the skeletal muscle alpha-actin (ACTA1) gene. Neuromuscular Disorders : Nmd. 11: 35-40
Jungbluth H, Sewry C, Brown SC, et al. (2000) Minicore myopathy in children: a clinical and histopathological study of 19 cases. Neuromuscular Disorders : Nmd. 10: 264-73
Mercuri E, Goodwin F, Sewry C, et al. (2000) Diaphragmatic spinal muscular atrophy with bulbar weakness. European Journal of Paediatric Neurology : Ejpn : Official Journal of the European Paediatric Neurology Society. 4: 69-72
Brockington M, Sewry CA, Herrmann R, et al. (2000) Assignment of a form of congenital muscular dystrophy with secondary merosin deficiency to chromosome 1q42. American Journal of Human Genetics. 66: 428-35
See more...